A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461620



Internal ID22519505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198832317..198834416hg38UCSC Ensembl
chr1:198801446..198803545hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829073
Supporting Variants
Samples
Known GenesMIR181A1HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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